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机构地区:[1]南京军区南京总医院中心仪器分析科
出 处:《药物分析杂志》1995年第5期17-19,共3页Chinese Journal of Pharmaceutical Analysis
摘 要:本文建立了用反相高效液相色谱法测定人血浆中双氯灭痛的方法,对样品提取及色谱分析条件等作了详细研究。血浆经酸化后用正己烷-异丙醇(95:5,V/V)提取,以SpherisorbC_(18)为固定相,甲醇与醋酸钠缓冲液的混合溶液(68:32,V/V;pH4.2)为流动相进行色谱分离。检测波长为274nm,二苯胺为内标。双氯灭痛浓度在0.10~2.50μg/ml范围内线性良好,r=0.9994。测定含双氯灭痛浓度为0.20μg/mi的血浆样品,其批内(n=9)及批间(n=7)相对标准偏差分别为7.4%和7.6%,回收率为91.3%~93.2%。应用本法测定了10名健康人口服双氯灭痛片剂后的体内血药浓度。Following a detailed study.a simple,rapid and accurate RP-HPLC method has been developed for the determination of diclofenac sodium in human plasma.The sample is separated isocratically within 7 min using an octadecyl-bonded silica column and a mobile phase of methanol and sodium acetate buffer(68:32.V/V.PH4.2).The compounds were quantitated using a ultraviolet detector operated at 274 nm which allowed determination of 0.10~2.50μg/ml of diclofenac sodium with high reproducibility.The limit of detection is 0.03μg/ml.Intraday and inter-day RSD for assaying the plasma sample containing0.20μg/ml concentration of diclofenac sodium were 7.4% (n=9)and 7.6%(n=7).respectively.The recoveries of diclofenac sodium were 91. 3% ~93. 2% for plasma.The method has been used to determine diclofenac sodium in plasma samples from ten volunteers and provide data on the pharmacokinetics of the drug.
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